Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,811 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,811 in last 12 months

Showing 3546135480 of 56,506 recalls

DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2016· Par Pharmaceutical, Inc.

Recalled Item: Travoprost Ophthalmic Solution USP Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Lack of Assurance of Sterility; damage to the internal portion of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C55¿ S61CM D66CM Catalog # AB101072 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Recalled...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S61CM D66CM GLOBAL...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...

The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C55¿ S79CM D84CM Catalog # AB081044 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· C.R. Bard, Inc.

Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....

The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...

The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C120¿ S61CM D66CM Catalog # AB081043 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...

The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C70¿ S79CM D84CM Catalog # AB081045 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C120¿ S79CM D84CM Catalog # AB081047 Recalled by...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Oscor, Inc.

Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C120¿ S61CM D66CM GLOBAL...

The Issue: Complaint that during insertion of the dilator through the sheath a fragment...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...

The Issue: The device defect is a positive bias of up to 20% relative to the currently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing